Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724375Generated: October 31, 2026

Sodium Bicarbonate → HCID 69373266, compound

https://huagongshe.com/reaction/724375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 69371688HCID 69371688—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69373266HCID 6937326640%

Reaction Conditions

Temperature60 °C

Reaction Steps

6-(1-Phenyl-vinyl)-3-styryl-1-[2-(trimethyl-silanyl)-ethoxymethyl]-1H-indazole (16.2 mg, 0.0358 mmol) was dissolved in THF (0.6 mL) and was treated with tetrabutylammonium fluoride (TBAF, 1M in THF, 0.6 mL). The mixture was heated to 60° C. under argon for 4 h. The mix was cooled, neutralized with excess saturated sodium bicarbonate and the organic material was extracted into ethyl acetate and concentrated. This mix of 3 compounds (by TLC visualization) was treated with THF water-TFA (1:1:2, 4 mL) for 30 min. The mix was diluted with toluene (20 mL), concentrated, neutralized with excess saturated sodium bicarbonate, and the organic material was extracted into ethyl acetate. The organic material was dried over sodium sulfate, decanted and concentrated. Purification by silica gel chromatography (2:8 ethyl acetate-hexane) gave 6-(1-Phenyl-vinyl)-3-styryl-1H-indazole (4.6 mg, 40%): Rf sm 0.62, p 0.24 (ethyl acetate-hexane 3:7); 1H NMR (300 MHz, CDCl3) δ 7.99 (d, 1H, J=8.5 Hz), 7.60–7.25 (m, 14H), 5.58 (d, 1H, J=1.1 Hz), 5.56 (d, 1H, J=1.1 Hz); HRMS (FAB) [m+H]/z Calc'd 323.1548. Found 323.1545.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141587B2
Source datasetuspto-grants-2006_11
ORD IDord-8fda33ed948e4a28b627a05f5a414e49
Source noteuspto-grants-2006_11